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HRID 12633作成日:2026年10月25日
Isopropanol → [1-(2-Amino-3-carbamoyl-phenylcarbamoyl)-cyclohexyl]-carbamic acid 9H-fluoren-9-ylmethyl ester
https://huagongshe.com/reaction/12633
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Isopropanol | HCID 3776 | — |
| 反応物 | 1-((Fmoc)amino)cyclohexanecarboxylic acid | HCID 2756093 | — |
| 反応物 | Bis-(1H-imidazol-2-YL)-methanone | HCID 5250894 | — |
| 反応物 | 2,3-Diaminobenzamide dihydrochloride | HCID 53422807 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | [1-(2-Amino-3-carbamoyl-phenylcarbamoyl)-cyclohexyl]-carbamic acid 9H-fluoren-9-ylmethyl ester | HCID 68508528 | — |
反応手順
A solution of 1-(9H-fluoren-9-ylmethoxycarbonyl amino)-cyclohexanecarboxylic acid (0.326 g, 0.9 mmol) in pyridine (1 mL) and DMF (1 ml) was heated to 40° C. for 30 min. Carbonyl diimidazole (0.15 g, 0.9 mmol) was added and the mixture was stirred at 40° C. for 1 hour then treated with 2,3-diamino-benzamide dihydrochloride (prepared as described in WO0026192, 0.2 g, 0.9 mmol). After stirring for 1 hour at room temperature, isopropyl alcohol (3 ml) was added and the solution was cooled overnight at 0° C. The precipitated solid was filtered, dissolved in water (3 ml), treated with 50% aqueous NaOH (0.071 ml) then stirred for 3 hours at room temperature. The mixture was filtered and used immediately in Example 48B.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07728026B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-3c7f730b94f942349c7865919bff10b4 |
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| 出典メモ | uspto-grants-2010_06 |
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